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肥厚性神经病神经活检标本中的脂质分析。

Lipid analysis in nerve biopsy specimens of hypertrophic neuropathy.

作者信息

Turpin J C, Hauw J J, Pollet S, Le Saux F, Escourolle R, Baumann N

出版信息

Arch Neurol. 1981 Jul;38(7):436-8. doi: 10.1001/archneur.1981.00510070070012.

DOI:10.1001/archneur.1981.00510070070012
PMID:6264902
Abstract

We performed a lipid analysis on nerve biopsy specimens in two cases of degenerative hypertrophic neuropathy. Quantitative analysis of the major lipid classes, ie, cholesterol, cerebrosides, sulfatides, ethanolamine phospholipids, phosphatidyl-choline, phosphatidyl-serine, phosphatidyl-inositol, sphingomyelin, and gangliosides, were performed. The two cases exhibited extreme decreases in levels of lipids that could be related to the very low myelin content of these nerves. Cholesterol and phospholipid levels were especially reduced. Cerebrosides and sulfatides were not modified in the same proportion, as could have been predicted from the degree of demyelination. This relative glycolipid increase could be due to the very high Schwann cell proliferation.

摘要

我们对两例退行性肥厚性神经病变患者的神经活检标本进行了脂质分析。对主要脂质类别,即胆固醇、脑苷脂、硫脂、乙醇胺磷脂、磷脂酰胆碱、磷脂酰丝氨酸、磷脂酰肌醇、鞘磷脂和神经节苷脂进行了定量分析。这两例患者的脂质水平极度降低,这可能与这些神经的髓鞘含量极低有关。胆固醇和磷脂水平尤其降低。脑苷脂和硫脂的变化比例与脱髓鞘程度的预期不同。这种相对糖脂增加可能是由于施万细胞的高度增殖。

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引用本文的文献

1
Hereditary motor and sensory neuropathy of demyelinating and remyelinating type in children. Ultrastructural and morphometric studies on sural nerve biopsy specimens from ten sporadic cases.儿童脱髓鞘和再髓鞘化型遗传性运动和感觉神经病。对10例散发病例腓肠神经活检标本的超微结构和形态计量学研究。
Acta Neuropathol. 1984;65(1):1-9. doi: 10.1007/BF00689822.